Lyric4 Hearing Aid

FDA 510(k) K232999 · Sonova AG

Substantially Equivalent

510(k) numberK232999

Submission

Device name
Lyric4 Hearing Aid
Applicant
Sonova AG
Staefa, CH
Received
September 22, 2023
Decision date
April 11, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ESD – Hearing Aid, Air-Conduction, Prescription
Device class
Class I (low risk)
Regulation
21 CFR 874.3300
Specialty
Ear, Nose, Throat

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.

Other 510(k)s with product code ESD

510(k)DeviceApplicantDecision
K130790LYRIC2ESD · Traditional Phonak, LLC06/27/2013SE
K081136Lyric Hearing AidESD · Traditional Insound Medical, Inc.05/08/2008SE
K021867Insound XT Series Hearing AidESD · Traditional Insound Medical, Inc.11/19/2002SE
K003558Tci Combi (Tinnitus Control Instrument Combination)ESD · Traditional Siemens Hearing Instruments, Inc.04/24/2001SE
K984518Sonic Innovations Completely-In-The-Canal DSP Hearing Aid with Soft ShellESD · Traditional Sonic Innovations, Inc.03/12/1999SE
K974751Tranquil Tri-Oe, Tranquil Tri-Coe, Tranquil Tri-CicESD · Traditional General Hearing Instruments, Inc.03/06/1998SE
K974242Argosy Programmable OnqueESD · Traditional Argosy Electronics01/20/1998SE
K973880Sonix Hearing Aid Fitting and Programming SystemESD · Traditional Sonix Technologies, Inc.01/12/1998SE
K974211Opus 2 - Full Concha Series - IteESD · Traditional Bernafon-Maico, Inc.12/15/1997SE
K974152Opus 2 - Completely-In-Canal Series (Cic)ESD · Traditional Bernafon-Maico, Inc.12/15/1997SE

More from Bernafon-Maico, Inc.

510(k)DeviceDecision
K230538All-Day Clear Slim ADCS1 Hearing Aid. All-Day Clear ADC1 Hearing AidQUH · Traditional 06/16/2023SE

Questions and answers

When was Lyric4 Hearing Aid cleared by the FDA?

Lyric4 Hearing Aid (K232999) received a 510(k) decision of Substantially Equivalent on April 11, 2024, 202 days after the submission was received.

What is the product code of K232999?

The FDA product code is ESD – Hearing Aid, Air-Conduction, Prescription, a Class I (low risk) device regulated under 21 CFR 874.3300.